211030-00-1

Basic information

• Product Name: (2Z,7Z)-2,8-bis(benzyloxycarbonylamino)nona-2,7-diene-1,9-dioic acid dimethyl ester
• Synonyms: (2Z,7Z)-2,8-bis(benzyloxycarbonylamino)nona-2,7-diene-1,9-dioic acid dimethyl ester
• CAS NO: 211030-00-1
• Molecular Weight: 510.544
• Mol File: 211030-00-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2Z,7Z)-2,8-bis(benzyloxycarbonylamino)nona-2,7-diene-1,9-dioic acid dimethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2Z,7Z)-2,8-bis(benzyloxycarbonylamino)nona-2,7-diene-1,9-dioic acid dimethyl ester(211030-00-1)
• EPA Substance Registry System: (2Z,7Z)-2,8-bis(benzyloxycarbonylamino)nona-2,7-diene-1,9-dioic acid dimethyl ester(211030-00-1)

Safety Data

• Hazardous Substances Data: 211030-00-1(Hazardous Substances Data)

Upstream product

• 100945-15-1 N-(benzyloxycarbonyl)phosphonoglycine trimethyl ester 
• 111-30-8 Glutaraldehyde 

Relevant articles and documents

Enantioselective synthesis of diamino dicarboxylic acids

The preparation of alkyl diamino dicarboxylic acids with high optical purity (100% ee, >98.5% de) and high yields based on asymmetric catalytic hydrogenation is described. The required prochiral precursors are prepared from dialdehydes and Z-, Boc-, and acetyl-protected phosphonoglycines. Aqueous solutions of glyoxal, succinic dialdehyde, and glutaric dialdehyde were used to prepare the diunsaturated precursors for 2,5-diaminoadipic acid (DAA), 2,7-diaminosuberic acid (DAS), and 2,8-diaminoazelaic acid (DAZ). Z- Protected dimethyl esters of DAA, DAS, and DAZ were obtained by hydrogenation of the corresponding prochiral starting materials with [(COD)Rh(S,S)- EtDuPHOS]OTf.